TRANSIENT IMMUNOGLOBULIN-M ANTIBODY-RESPONSE TO HEPATITIS-C VIRUS CAPSID ANTIGEN IN POSTTRANSFUSION HEPATITIS-C - PUTATIVE SEROLOGICAL MARKER FOR ACUTE VIRAL-INFECTION

被引:64
作者
CHEN, PJ
WANG, JT
HWANG, LH
YANG, YH
HSIEH, CL
KAO, JH
SHEU, JC
LAI, MY
WANG, TH
CHEN, DS
机构
[1] NATL TAIWAN UNIV HOSP,HEPATITIS RES CTR,1 CHANG TE ST,TAIPEI 100,TAIWAN
[2] NATL TAIWAN UNIV HOSP,GRAD INST CLIN MED,TAIPEI 100,TAIWAN
[3] NATL TAIWAN UNIV HOSP,DEPT INTERNAL MED,TAIPEI 100,TAIWAN
[4] NATL TAIWAN UNIV,COLL MED,TAIPEI,TAIWAN
[5] DEV CTR BIOTECHNOL,DIV MOLEC BIOL,TAIPEI,TAIWAN
关键词
RNA VIRUS; CHRONIC INFECTION;
D O I
10.1073/pnas.89.13.5971
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The development of serological assays for hepatitis C virus (HCV) has made specific diagnosis possible. However, markers useful in indicating acute-phase HCV infection have not been identified. By an immunoblotting method, we characterized the IgM and IgG antibody response against HCV capsid antigen in patients with HCV infection. Among 88% of patients with acute posttransfusion hepatitis C recruited in a prospective study, there was a transient IgM antibody response. The IgM antibody appeared shortly after onset of hepatitis (average 3.7 weeks), persisted for several months (average 18 weeks), and then disappeared. In contrast, the IgG antibody persisted long-term once it appeared. Among patients with chronic hepatitis C with milder disease activities (serum aminotransferase increase above normal levels of <4-fold), the IgM antibody was negative in the majority (72%). In those with acute exacerbations (aminotransferase increase of >10-fold), about 55% were negative for the IgM antibody. The reactivity of the IgM antibody in the rest was weaker or became negative upon further dilution of serum. The results suggest that IgM anti-capsid antibody may serve as a marker indicating acute or active HCV infection.
引用
收藏
页码:5971 / 5975
页数:5
相关论文
共 25 条
[1]   DETECTION OF ANTIBODY TO HEPATITIS-C VIRUS IN PROSPECTIVELY FOLLOWED TRANSFUSION RECIPIENTS WITH ACUTE AND CHRONIC NON-A-HEPATITIS, NON-B-HEPATITIS [J].
ALTER, HJ ;
PURCELL, RH ;
SHIH, JW ;
MELPOLDER, JC ;
HOUGHTON, M ;
CHOO, QL ;
KUO, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 321 (22) :1494-1500
[2]   THE HEPATITIS-C VIRUS AND ITS RELATIONSHIP TO THE CLINICAL SPECTRUM OF NANB HEPATITIS [J].
ALTER, HJ .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1990, 5 :78-94
[3]  
ALTER HJ, 1984, VIRAL HEPATITIS LIVE, P345
[4]   RISK-FACTORS FOR ACUTE NON-A, NON-B HEPATITIS IN THE UNITED-STATES AND ASSOCIATION WITH HEPATITIS-C VIRUS-INFECTION [J].
ALTER, MJ ;
HADLER, SC ;
JUDSON, FN ;
MARES, A ;
ALEXANDER, WJ ;
HU, PY ;
MILLER, JK ;
MOYER, LA ;
FIELDS, HA ;
BRADLEY, DW ;
MARGOLIS, HS .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1990, 264 (17) :2231-2235
[5]  
BURNETTE WN, 1981, ANAL BIOCHEM, V112, P195, DOI 10.1016/0003-2697(81)90281-5
[6]   ISOLATION OF A COMPLEMENTARY-DNA FRAGMENT OF HEPATITIS-C VIRUS IN TAIWAN REVEALED SIGNIFICANT SEQUENCE VARIATIONS COMPARED WITH OTHER ISOLATES [J].
CHEN, PJ ;
LIN, MH ;
TU, SJ ;
CHEN, DS .
HEPATOLOGY, 1991, 14 (01) :73-78
[7]   IGM ANTIBODY-RESPONSE IN ACUTE HEPATITIS-C VIRAL-INFECTION [J].
CLEMENS, JM ;
TASKAR, S ;
CHAU, K ;
VALLARI, D ;
SHIH, JWK ;
ALTER, HJ ;
SCHLEICHER, JB ;
MIMMS, LT .
BLOOD, 1992, 79 (01) :169-172
[8]   LONG-TERM CLINICAL AND HISTOPATHOLOGICAL FOLLOW-UP OF CHRONIC POSTTRANSFUSION HEPATITIS [J].
DIBISCEGLIE, AM ;
GOODMAN, ZD ;
ISHAK, KG ;
HOOFNAGLE, JH ;
MELPOLDER, JJ ;
ALTER, HJ .
HEPATOLOGY, 1991, 14 (06) :969-974
[9]   DIAGNOSIS OF ACUTE AND INAPPARENT HEPATITIS-B VIRUS-INFECTIONS BY MEASUREMENT OF IGM ANTIBODY TO HEPATITIS-B CORE ANTIGEN [J].
GERLICH, WH ;
LUER, W ;
THOMSSEN, R .
JOURNAL OF INFECTIOUS DISEASES, 1980, 142 (01) :95-101
[10]  
HAJIKATA M, 1991, P NATL ACAD SCI USA, V88, P5547